Enhance your expertise at AtomVie Global Radiopharma as a Quality Assurance Associate Systems in Hamilton, ON. This role focuses on ensuring compliance with GMP standards in radiopharmaceutical manufacturing.
You will serve as a vital link between quality assurance, production, and regulatory teams, ensuring all activities are compliant with established protocols. Your role includes conducting audits, mentoring QA staff, and managing critical documentation processes, all pivotal for the advancement of cancer therapies.
Key Responsibilities:
• Ensure quality systems adhere to GMP regulations
• Lead and participate in internal and regulatory audits
• Manage change controls and CAPAs effectively
• Prepare audits, reports, and metrics for management
• Provide training to new employees on quality processes
Requirements:
• Degree in Engineering, Microbiology, or related field
• 3-5 years of relevant quality assurance experience
• Familiarity with GMP regulat...